Job Search and Career Advice Platform

Enable job alerts via email!

Informatics Analyst II

Premier Research Group

Remote

GBP 45,000 - GBP 60,000

Full time

Today
Be an early applicant

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Job summary

A leading clinical research company in the United Kingdom is looking for an Informatics Analyst II. This role involves reviewing data for proposals, designing feasibility questionnaires, and compiling reports to support project delivery. Candidates should hold relevant degrees and possess at least two years of experience in clinical trials or informatics. Strong communication skills and familiarity with clinical databases are essential. Join a team dedicated to transforming lives through innovative research.

Benefits

Continuous learning opportunities
Innovative technologies
Flexible work environment

Qualifications

  • Minimum undergraduate degree in a related field.
  • 2+ years’ experience in a global Feasibility/Informatics role.
  • Experience in clinical trials or pharmaceutical industry essential.

Responsibilities

  • Review internal and external data to support RFP.
  • Design feasibility questionnaires and analyze data.
  • Compile and recommend country selections for proposals.

Skills

Excellent verbal and written English communication
Data analysis skills
Clinical trial knowledge

Education

Undergraduate degree in a clinical, biological, or health-related field
Postgraduate degree (MSc, MPhil or PhD)

Tools

Clinical Trial Databases (e.g. Citeline)
Job description
Informatics Analyst II page is loaded## Informatics Analyst IIremote type: Remotelocations: United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R5918Premier Research is looking for a Informatics Analyst II to join our Business Operations team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.* We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.* Your ideas influence the way we work, and your voice matters here.* As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.Join us and build your future here.**What You’ll Be Doing:*** Review internal data and external literature to obtain a background understanding of Premier Research experience, country specific treatment patterns, available medications and competitive studies/market for disease areas to support Request For Proposal (RFP)* Design protocol specific site-level electronic feasibility questionnaires to collect metrics-based data, collate responses and analyse data to provide regularly updated summary report to proposal team for review* Compile the data into a report based on available data, together with the study team, make a recommendation on country selection, type of sites, numbers of sites, number of patients per country and recruitment timelines for inclusion in the proposal* Identify key information to be collated from local Study Start-Up Associates to support country strategy development* Write up medical informatics results and recommendations on strategic patient recruitment plan for inclusion in proposals and/or feasibility reports and bid defense slides* Undertake scientific literature reviews in collaboration with the medical strategist to understand treatment patterns, guidelines, standards of care and available medications for therapeutic disease areas within sponsor areas of focus.* Identify patient sources and flow, i.e. diagnosis, referral and treatment/care pathways in each country, to support the proposal bid and ultimately the project delivery post award.* Use computer-based models to project patient recruitment in studies, tailored to protocol design and country/site distribution**What We Are Searching For:*** Minimum undergraduate degree in a clinical, biological, scientific, or health-related field, preferred postgraduate degree (MSc, MPhil or PhD) in a clinical, biological, scientific, or health-related field.* 2+ years’ experience in a global Feasibility/Informatics related role required.* Prior clinical trials support or pharmaceutical industry experience is required.* Experience using external Clinical Trial Databases (e.g. Citeline) is highly desirable.* Excellent verbal and written English communication and presentation skills, demonstrating credibility in customer-facing situations.* Premier Research is more than a company – it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems.* Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies.* As a Premier team member, you have the power to make an impact, regardless of job title and location.* Our dedication to biotech and specialty pharma is unlike any other.* We provide our staff with innovative technologies and continuous learning.### Join Our NetworkIntroduce yourself to our Talent Team and we will reach out if there is a role that aligns with your experience and interests.Premier Research is a global clinical research, product development, and consulting company. We are dedicated to helping biotech, specialty pharma, and MedTech innovators transform life-changing ideas and breakthrough science into new medical treatments. Our team is inspired by this common purpose. Premier is a place where you can change lives, and feel rewarded and celebrated. We aim high - we will not stop until we reach our goals. And we care about each other, about our customer and partners, and, most importantly, about all the patients that we touch with our work.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

CRA 2 - Single Sponsor Dedicated

IQVIA

Livingston
On-site
GBP 30,000 - 45,000
Full time
30+ days ago
Dedicated Line Manager, sponsor-dedicated

IQVIA

Reading
On-site
GBP 45,000 - 60,000
Full time
30+ days ago
Sr. CRA 1 - Single Sponsor Dedicated

IQVIA

United Kingdom
On-site
GBP 60,000 - 80,000
Full time
30+ days ago
Specialist, Clinical Trials

Neurocrine Biosciences, Inc.

Greater London
Hybrid
GBP 35,000 - 50,000
Full time
30+ days ago
Data Team Lead - homebased (FSP)

IQVIA

England
Hybrid
GBP 50,000 - 70,000
Full time
30+ days ago
Experienced CRA - Single Sponsor Dedicated

IQVIA

United Kingdom
On-site
GBP 60,000 - 80,000
Full time
30+ days ago
Clinical Trials Specialist

Neurocrine Biosciences, Inc.

Greater London
On-site
GBP 40,000 - 55,000
Full time
30+ days ago
Clinical FSP Quality Manager

IQVIA

Reading
Hybrid
GBP 45,000 - 60,000
Full time
30+ days ago
Operations Specialist

IQVIA

Greater London
On-site
GBP 60,000 - 80,000
Full time
30+ days ago
Senior Consultant – Global Pricing & Market Access

Clarivate Analytics

Greater London
Hybrid
GBP 70,000 - 90,000
Full time
30+ days ago